Evidence map›Paper›PMID 25422494›Full record

ArticleThe Journal of experimental medicine2014

Cytomegalovirus generates long-lived antigen-specific NK cells with diminished bystander activation to heterologous infection.

Gundula Min-Oo, Lewis L Lanier

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
6.0field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

67 citing papers in PubMed, 106 citations in OpenAlex.

  1. NK Cell Activity and CD57Frontiers in immunology · 2020
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  20. Virus-specific NK cell memory.The Journal of experimental medicine · 2021
    Review

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

Gundula Min-OoDepartment of Microbiology and Immunology and Cancer Research Institute, University of California San Francisco, San Francisco, CA 94143 Department of Microbiology and Immunology and Cancer Research Institute, University of California San Francisco, San Francisco, CA 94143.
Lewis L LanierDepartment of Microbiology and Immunology and Cancer Research Institute, University of California San Francisco, San Francisco, CA 94143 Department of Microbiology and Immunology and Cancer Research Institute, University of California San Francisco, San Francisco, CA 94143 Lewis.Lanier@ucsf.edu.
Cancer Research Institute · USUniversity of California, San Francisco · US

Funding

UCSF Liver Core CenterP30DK026743 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Holger Willenbring · 1986 to 2026
$30.7M
NK MemoryR01AI068129 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LANIER, LEWIS LEE · 2006 to 2020
$6.0M
NIAID NIH HHS AI068129NIAID NIH HHS R01 AI068129NIDDK NIH HHS P30 DK026743
6 · The paper itself

Abstract

Natural killer (NK) cells play a key role in the host response to cytomegalovirus (CMV) and can mediate an enhanced response to secondary challenge with CMV. We assessed the ability of mouse CMV (MCMV)-induced memory Ly49H(+) NK cells to respond to challenges with influenza, an acute viral infection localized to the lung, and Listeria monocytogenes, a systemic bacterial infection. MCMV-memory NK cells did not display enhanced activation or proliferation after infection with influenza or Listeria, as compared with naive Ly49H(+) or Ly49H(-) NK cells. Memory NK cells also showed impaired activation compared with naive cells when challenged with a mutant MCMV lacking m157, highlighting their antigen-specific response. Ex vivo, MCMV-memory NK cells displayed reduced phosphorylation of STAT4 and STAT1 in response to stimulation by IL-12 and type I interferon (IFN), respectively, and IFN-γ production was reduced in response to IL-12 + IL-18 compared with naive NK cells. However, costimulation of MCMV-memory NK cells with IL-12 and m157 antigen rescues their impaired response compared with cytokines alone. These findings reveal that MCMV-primed memory NK cells are diminished in their response to cytokine-driven bystander responses to heterologous infections as they become specialized and antigen-specific for the control of MCMV upon rechallenge.

Indexed as

Adoptive TransferAnimalsAntigens, ViralBystander EffectCell ProliferationCytokinesDisease Models, AnimalDogsEpitopesFemaleHerpesviridae InfectionsImmunologic MemoryInfluenza A Virus, H1N1 SubtypeKiller Cells, NaturalListeriosisLymphocyte ActivationAntigens, ViralCytokinesEpitopesNK Cell Lectin-Like Receptor Subfamily AReceptors, Cytokine

Identifiers

PMID25422494
PMCPMC4267234
OpenAlexW2157191688

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.